Suppr超能文献

酒石酸 eliglustat,一种典型的葡萄糖神经酰胺合酶抑制剂。

Eliglustat tartrate, a prototypic glucosylceramide synthase inhibitor.

作者信息

Shayman James A

机构信息

a Department of Internal Medicine, University of Michigan Medical School, 1150 West Medical Center Drive, Ann Arbor, Michigan 48109, USA

出版信息

Expert Rev Endocrinol Metab. 2013 Nov;8(6):491-504. doi: 10.1586/17446651.2013.846213.

Abstract

Eliglustat tartrate is a highly specific inhibitor of glucosylceramide synthase, developed for the treatment glucosylceramide-based glycosphingolipidoses. Eliglustat is in late clinical development for Gaucher disease type 1. Phase II and III clinical trials have demonstrated clinical efficacy for eliglustat as a stand-alone agent for newly diagnosed patients that are naïve to prior therapy and for patients who have been previously treated with enzyme replacement therapy. Importantly, the reported toxicity of eliglustat has been limited. Eliglustat will be submitted for the US FDA and EMA review in late 2013. Several structurally unrelated glucosylceramide synthase inhibitors have been identified and are in various stages of development, some of which cross the blood-brain barrier. Targeting glucosylceramide synthesis is also a promising approach for the treatment of type 2 diabetes mellitus, autosomal dominant polycystic kidney disease and certain cancers.

摘要

酒石酸艾立布林是葡糖神经酰胺合酶的一种高度特异性抑制剂,开发用于治疗基于葡糖神经酰胺的糖鞘脂贮积症。艾立布林正处于1型戈谢病的临床后期开发阶段。II期和III期临床试验已证明艾立布林作为新诊断的未接受过先前治疗的患者以及先前接受过酶替代治疗的患者的单一治疗药物具有临床疗效。重要的是,已报道的艾立布林毒性有限。艾立布林将于2013年末提交美国食品药品监督管理局(FDA)和欧洲药品管理局(EMA)审评。已鉴定出几种结构不相关的葡糖神经酰胺合酶抑制剂,它们处于不同的开发阶段,其中一些可穿过血脑屏障。靶向葡糖神经酰胺合成也是治疗2型糖尿病、常染色体显性多囊肾病和某些癌症的一种有前景的方法。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验